Formation of corneal endothelium is essential for anterior segment development - a transgenic mouse model of anterior segment dysgenesis

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				S.-W. M. Koh, K. Chandrasekara, C. J. Abbondandolo, T. J. Coll, and A. R. Rutzen VIP and VIP Gene Silencing Modulation of Differentiation Marker N-Cadherin and Cell Shape of Corneal Endothelium in Human Corneas Ex Vivo Invest. Ophthalmol. Vis. Sci., August 1, 2008; 49(8): 3491 - 3498. [Abstract] [Full Text] [PDF]

				L. Hansen, W. Yao, H. Eiberg, K. W. Kjaer, K. Baggesen, J. F. Hejtmancik, and T. Rosenberg Genetic Heterogeneity in Microcornea-Cataract: Five Novel Mutations in CRYAA, CRYGD, and GJA8 Invest. Ophthalmol. Vis. Sci., September 1, 2007; 48(9): 3937 - 3944. [Abstract] [Full Text] [PDF]

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				U. Hopfer, N. Fukai, H. Hopfer, G. Wolf, N. Joyce, E. Li, and B. R. Olsen Targeted disruption of Col8a1 and Col8a2 genes in mice leads to anterior segment abnormalities in the eye FASEB J, August 1, 2005; 19(10): 1232 - 1244. [Abstract] [Full Text] [PDF]

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				J. Davis, M. K. Duncan, W. G. Robison Jr, and J. Piatigorsky Requirement for Pax6 in corneal morphogenesis: a role in adhesion J. Cell Sci., June 1, 2003; 116(11): 2157 - 2167. [Abstract] [Full Text] [PDF]

				M. A. Lines, K. Kozlowski, and M. A. Walter Molecular genetics of Axenfeld-Rieger malformations Hum. Mol. Genet., May 15, 2002; 11(10): 1177 - 1187. [Abstract] [Full Text] [PDF]

				D. B. Gould and S. W. M. John Anterior segment dysgenesis and the developmental glaucomas are complex traits Hum. Mol. Genet., May 15, 2002; 11(10): 1185 - 1193. [Abstract] [Full Text] [PDF]

				H. M. Espinoza, C. J. Cox, E. V. Semina, and B. A. Amendt A molecular basis for differential developmental anomalies in Axenfeld-Rieger syndrome Hum. Mol. Genet., April 1, 2002; 11(7): 743 - 753. [Abstract] [Full Text] [PDF]

				Y. Ueda, M. K. Duncan, and L. L. David Lens Proteomics: The Accumulation of Crystallin Modifications in the Mouse Lens with Age Invest. Ophthalmol. Vis. Sci., January 1, 2002; 43(1): 205 - 215. [Abstract] [Full Text] [PDF]

				M. Giovannini, E. Robanus-Maandag, M. van der Valk, M. Niwa-Kawakita, V. Abramowski, L. Goutebroze, J. M. Woodruff, A. Berns, and G. Thomas Conditional biallelic Nf2 mutation in the mouse promotes manifestations of human neurofibromatosis type 2 Genes & Dev., July 1, 2000; 14(13): 1617 - 1630. [Abstract] [Full Text]